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Heparin as a molecular spacer immobilized on microspheres to improve blood compatibility in hemoperfusion
Carbohydrate Polymers ( IF 11.2 ) Pub Date : 2018-09-01 , DOI: 10.1016/j.carbpol.2018.08.067
Qi Dang , Chun-Gong Li , Xin-Xin Jin , Ya-Jin Zhao , Xiang Wang

Heparin, a highly sulfated linear polysaccharide, with anticoagulation function and blood compatibility is widely used as a biomaterials in medical application, but the most importance of heparin is its structure function as the macromolecular space arm. In this study, heparin as a spacer was covalently immobilized on the chloromethylated polystyrene microspheres (Ps) and then connected with L-phenylalanine forming the Ps-Hep-Phe structure, which was developed for endotoxin adsorption in hemoperfusion. The grafting density of heparin reach the maximum when the initial concentration of heparin solution was 5mg/mL. The adsorbents with the heparin as a spacer showed the prolonged clotting times, low protein adsorption, and reduced the hemolysis rate, indicating that heparin-modified adsorbents have great blood compatibility. The adsorption capacity of Ps-Hep-Phe for endotoxin was 25.15EU/g in dynamic adsorption, higher than that of Ps. Therefore, this study imply that heparin would be promising for modification of adsorbents in hemoperfusion.



中文翻译:

肝素作为固定在微球上的分子间隔物,可改善血液灌流中的血液相容性

肝素是一种高度硫酸化的线性多糖,具有抗凝功能和血液相容性,在医学应用中被广泛用作生物材料,但是肝素最重要的是其作为大分子空间臂的结构功能。在这项研究中,肝素作为间隔物被共价固定在氯甲基化的聚苯乙烯微球(Ps)上,然后与L-苯丙氨酸连接形成Ps- Hep-Phe结构,专为血液灌流中的内毒素吸附而开发。当肝素溶液的初始浓度为5mg / mL时,肝素的接枝密度达到最大值。以肝素为间隔物的吸附剂显示出延长的凝血时间,较低的蛋白质吸附和降低的溶血速率,表明肝素修饰的吸附剂具有良好的血液相容性。动态吸附中Ps-Hep-Phe对内毒素的吸附能力为25.15EU / g,高于Ps。因此,这项研究表明肝素有望在血液灌流中修饰吸附剂。

更新日期:2018-09-03
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